Search results
Results from the WOW.Com Content Network
Imazaquin along with imazamethabenz-methyl, imazapyr, imazapic, imazethapyr, and imazamox comprise the class of synthetic compounds termed the imidazolinone herbicides. These chemicals all feature an imidazolinone ring with a carboxylic acid group attached to the backbone. [4] They vary in the attached ring structure.
Imazapic is a chemical used as an herbicide. It controls many broad leaf weeds and controls or suppresses some grasses in pasture, rangeland and certain types of turf. It has a half-life of around 120 days in soil. [1] [2] Imazapic is considered an environmental hazard due to its harmful effects on aquatic life. [3]
Imazapyr is an ingredient of the commercial product Ortho GroundClear. A related herbicide, imazapic is an ingredient in Roundup Extended Control. Both chemicals are non-selective, long-lasting, and effective in weed control.
The ammonium ion is generated when ammonia, a weak base, reacts with Brønsted acids (proton donors): H + + NH 3 → [NH 4] + The ammonium ion is mildly acidic, reacting with Brønsted bases to return to the uncharged ammonia molecule: [NH 4] + + B − → HB + NH 3. Thus, the treatment of concentrated solutions of ammonium salts with a strong ...
Ammonium hexachlorostannate (also known as pink salt) is an inorganic chemical compound with the chemical formula (NH 4) 2 SnCl 6. [1] [2] [3]
6 These form water-stable salts. [12] The anion has an ethane-like structure and contains a P−P bond. The formal oxidation state of phosphorus is +4. The oxygen analogue is the hypodiphosphate anion, P 2 O 4− 6. P 3 S 3− 9 contains a six-membered P 3 S 3 ring. The ammonium salt is produced by reaction of P 4 S 10 in liquid ammonia. [13]
propanoic acid, ammonium salt(1:1) ... It has the chemical formula NH 4 (C 2 H 5 COO). Reaction. It is formed by the reaction of propionic acid and ammonia. Uses
Aliquat 336 is used as a phase transfer catalyst, [2] including in the catalytic oxidation of cyclohexene to 1,6-hexanedioic acid. [3] This reaction is an example of green chemistry, as it is more environmentally friendly than the traditional method of oxidizing cyclohexanol or cyclohexanone with nitric acid or potassium permanganate, which produce hazardous wastes.